The following data is part of a premarket notification filed by Philips Medizinsysteme Boblingen Gmbh with the FDA for The Philips Mp20,mp30,mp40,mp50,mp60,mp70,mp80 And Mp90 Intellivue Atient Monitors.
| Device ID | K060541 |
| 510k Number | K060541 |
| Device Name: | THE PHILIPS MP20,MP30,MP40,MP50,MP60,MP70,MP80 AND MP90 INTELLIVUE ATIENT MONITORS |
| Classification | Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) |
| Applicant | PHILIPS MEDIZINSYSTEME BOBLINGEN GMBH HEWLETT PACKARD STR. 2 Boblingen, DE D 71034 |
| Contact | Herbert Van Dyk |
| Correspondent | Herbert Van Dyk PHILIPS MEDIZINSYSTEME BOBLINGEN GMBH HEWLETT PACKARD STR. 2 Boblingen, DE D 71034 |
| Product Code | MHX |
| Subsequent Product Code | BZQ |
| Subsequent Product Code | CBQ |
| Subsequent Product Code | CBR |
| Subsequent Product Code | CBS |
| Subsequent Product Code | CCK |
| Subsequent Product Code | CCL |
| Subsequent Product Code | NHO |
| Subsequent Product Code | NHP |
| Subsequent Product Code | NHQ |
| CFR Regulation Number | 870.1025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-03-01 |
| Decision Date | 2006-03-24 |
| Summary: | summary |